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A case of Lujan-Fryns syndromes

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dc.creator Dundar, Nihal Olgac
dc.creator Dundar, Bumin Nuri
dc.creator Akkaya, Ayca Esra
dc.date 2010-09-01T00:00:00Z
dc.date.accessioned 2021-12-03T11:32:16Z
dc.date.available 2021-12-03T11:32:16Z
dc.identifier 92ab4413-48ac-4db9-ae0e-23b691f8910d
dc.identifier 10.4274/tpa.45.291
dc.identifier https://avesis.sdu.edu.tr/publication/details/92ab4413-48ac-4db9-ae0e-23b691f8910d/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/93370
dc.description The Lujan-Fryns syndrome (X-linked mental retardation with marfanoid habitus syndrome) is an X-linked form of syndromal mental retardation affecting predominantly males. The prevalence is not known. The syndrome is associated with mild to moderate mental retardation, distinct facial dysmorphism, marfanoid stature, long slender extremities, and behavioural problems. The diagnosis is based on the presence of the clinical manifestations. Here, we presented a 14 years and 2 months boy old boy who applied our outpatient clinic with the complaint of high stature (height SDS:3.45) and diagnosed as Lujan-Fryns syndrome with the detection of physical findings such as mental retarded appearence, poor eye contact, long face, small chin, molar hypoplasia, high and narrow palate, hypernasal speech, pectus carinatum, pes planus and long extremities and fingers. (Turk Arch Ped 2010; 45: 291-4)
dc.language tur
dc.rights info:eu-repo/semantics/openAccess
dc.title A case of Lujan-Fryns syndromes
dc.type info:eu-repo/semantics/article


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